[Retracted] Analysis of Clinical Manifestations, Imaging Features, and Gene Mutation Characteristics of 6 Children with Cystic Fibrosis in China

Table 1

Clinical manifestations and laboratory test results of 6 children with CF.

Case	Gender	Age ofonset	Age of diagnosis	Main clinical manifestations	Pathogenicbacteria	Sweat chlorineconcentration (mmol/L)
Case 1	Male	2 months	5 months	Repeated respiratory tract infections, diarrhea, celiac disease, liver dysfunction, sweat crystals, moderate obstructive ventilatory dysfunction	Pseudomonas aeruginosa	140
Case 2	Male	7 months	2 years	Repeated respiratory tract infections, liver dysfunction, moderate-to-severe obstructive ventilatory dysfunction	Pseudomonas aeruginosa	110
Case 3	Female	3 months	5 months	Repeated respiratory tract infection, diarrhea, fatty diarrhea, abnormal liver function, normal lung function, growth retardation	Staphylococcus aureus	Not checked
Case 4	Male	12 days	9 months	Repeated respiratory tract infections, diarrhea, celiac disease, PBS, moderate obstructive ventilatory dysfunction	Staphylococcus aureus	Not checked
Case 5	Female	3 days	4 months	It begins with cholestasis, manifested as jaundice and abnormal liver function.	Not checked	Not checked
Case 6	Male	1 month	1 year	Repeated respiratory tract infections, combined with PBS, mild obstructive ventilatory dysfunction	Pseudomonas aeruginosa	Not checked